Diagnostic Biopsy via In-Office Frozen Sections for Clinical Nonmelanoma Skin Cancer

BACKGROUND Treatment of nonmelanoma skin cancer (NMSC) by Mohs surgery has traditionally relied on previous pathologic evaluation of paraffin-embedded tissue. Tissue processing by frozen sections allows for expedited diagnosis and treatment; however, data on its accuracy are limited. OBJECTIVE To me...

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Veröffentlicht in:Dermatologic surgery 2021-02, Vol.47 (2), p.194-199
Hauptverfasser: Mulvaney, Patrick M., Piris, Adriano, Besaw, Robert J., Schmults, Chrysalyne D.
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container_issue 2
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container_title Dermatologic surgery
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creator Mulvaney, Patrick M.
Piris, Adriano
Besaw, Robert J.
Schmults, Chrysalyne D.
description BACKGROUND Treatment of nonmelanoma skin cancer (NMSC) by Mohs surgery has traditionally relied on previous pathologic evaluation of paraffin-embedded tissue. Tissue processing by frozen sections allows for expedited diagnosis and treatment; however, data on its accuracy are limited. OBJECTIVE To measure the accuracy and outcomes of biopsy via frozen sections for clinical NMSC. METHODS Biopsies of clinical NMSCs processed via frozen sections with in-office diagnosis rendered by one Mohs surgeon were retrospectively reviewed by one board-certified dermatopathologist. Discordant diagnoses were re-read in blinded fashion by both physicians. If still discordant, final diagnosis was determined by consensus discussion. Inter-rater reliability was calculated using Cohen's kappa statistic. RESULTS Two hundred ninety-seven lesions from 208 patients were included. Correlation between in-office and final diagnosis was 0.876 indicating "almost perfect" concordance. Sensitivity and specificity of in-office diagnosis for detecting malignancy were 98.1% and 94.4%. Seven cases (2.0%) had a clinically relevant change in final diagnosis, but appropriate treatment had been rendered. Two benign lesions (0.7%) initially diagnosed as malignant underwent excision. CONCLUSION In-office biopsy via frozen sections is highly accurate in confirming NMSC. This practice may speed diagnosis and treatment thus improving outcomes and patient satisfaction.
doi_str_mv 10.1097/DSS.0000000000002473
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Tissue processing by frozen sections allows for expedited diagnosis and treatment; however, data on its accuracy are limited. OBJECTIVE To measure the accuracy and outcomes of biopsy via frozen sections for clinical NMSC. METHODS Biopsies of clinical NMSCs processed via frozen sections with in-office diagnosis rendered by one Mohs surgeon were retrospectively reviewed by one board-certified dermatopathologist. Discordant diagnoses were re-read in blinded fashion by both physicians. If still discordant, final diagnosis was determined by consensus discussion. Inter-rater reliability was calculated using Cohen's kappa statistic. RESULTS Two hundred ninety-seven lesions from 208 patients were included. Correlation between in-office and final diagnosis was 0.876 indicating "almost perfect" concordance. Sensitivity and specificity of in-office diagnosis for detecting malignancy were 98.1% and 94.4%. Seven cases (2.0%) had a clinically relevant change in final diagnosis, but appropriate treatment had been rendered. Two benign lesions (0.7%) initially diagnosed as malignant underwent excision. CONCLUSION In-office biopsy via frozen sections is highly accurate in confirming NMSC. 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Tissue processing by frozen sections allows for expedited diagnosis and treatment; however, data on its accuracy are limited. OBJECTIVE To measure the accuracy and outcomes of biopsy via frozen sections for clinical NMSC. METHODS Biopsies of clinical NMSCs processed via frozen sections with in-office diagnosis rendered by one Mohs surgeon were retrospectively reviewed by one board-certified dermatopathologist. Discordant diagnoses were re-read in blinded fashion by both physicians. If still discordant, final diagnosis was determined by consensus discussion. Inter-rater reliability was calculated using Cohen's kappa statistic. RESULTS Two hundred ninety-seven lesions from 208 patients were included. Correlation between in-office and final diagnosis was 0.876 indicating "almost perfect" concordance. Sensitivity and specificity of in-office diagnosis for detecting malignancy were 98.1% and 94.4%. Seven cases (2.0%) had a clinically relevant change in final diagnosis, but appropriate treatment had been rendered. Two benign lesions (0.7%) initially diagnosed as malignant underwent excision. CONCLUSION In-office biopsy via frozen sections is highly accurate in confirming NMSC. 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numerical data</topic><topic>Humans</topic><topic>Keratosis, Actinic - diagnosis</topic><topic>Keratosis, Actinic - pathology</topic><topic>Keratosis, Actinic - surgery</topic><topic>Life Sciences &amp; Biomedicine</topic><topic>Male</topic><topic>Mohs Surgery - statistics &amp; numerical data</topic><topic>Observer Variation</topic><topic>Reproducibility of Results</topic><topic>Retrospective Studies</topic><topic>Science &amp; Technology</topic><topic>Skin - pathology</topic><topic>Skin Neoplasms - diagnosis</topic><topic>Skin Neoplasms - pathology</topic><topic>Skin Neoplasms - surgery</topic><topic>Surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mulvaney, Patrick M.</creatorcontrib><creatorcontrib>Piris, Adriano</creatorcontrib><creatorcontrib>Besaw, Robert J.</creatorcontrib><creatorcontrib>Schmults, Chrysalyne D.</creatorcontrib><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Web of Science - Science Citation Index Expanded - 2021</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Dermatologic surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mulvaney, Patrick M.</au><au>Piris, Adriano</au><au>Besaw, Robert J.</au><au>Schmults, Chrysalyne D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diagnostic Biopsy via In-Office Frozen Sections for Clinical Nonmelanoma Skin Cancer</atitle><jtitle>Dermatologic surgery</jtitle><stitle>DERMATOL SURG</stitle><addtitle>Dermatol Surg</addtitle><date>2021-02-01</date><risdate>2021</risdate><volume>47</volume><issue>2</issue><spage>194</spage><epage>199</epage><pages>194-199</pages><issn>1076-0512</issn><eissn>1524-4725</eissn><abstract>BACKGROUND Treatment of nonmelanoma skin cancer (NMSC) by Mohs surgery has traditionally relied on previous pathologic evaluation of paraffin-embedded tissue. Tissue processing by frozen sections allows for expedited diagnosis and treatment; however, data on its accuracy are limited. OBJECTIVE To measure the accuracy and outcomes of biopsy via frozen sections for clinical NMSC. METHODS Biopsies of clinical NMSCs processed via frozen sections with in-office diagnosis rendered by one Mohs surgeon were retrospectively reviewed by one board-certified dermatopathologist. Discordant diagnoses were re-read in blinded fashion by both physicians. If still discordant, final diagnosis was determined by consensus discussion. Inter-rater reliability was calculated using Cohen's kappa statistic. RESULTS Two hundred ninety-seven lesions from 208 patients were included. Correlation between in-office and final diagnosis was 0.876 indicating "almost perfect" concordance. Sensitivity and specificity of in-office diagnosis for detecting malignancy were 98.1% and 94.4%. Seven cases (2.0%) had a clinically relevant change in final diagnosis, but appropriate treatment had been rendered. Two benign lesions (0.7%) initially diagnosed as malignant underwent excision. CONCLUSION In-office biopsy via frozen sections is highly accurate in confirming NMSC. This practice may speed diagnosis and treatment thus improving outcomes and patient satisfaction.</abstract><cop>PHILADELPHIA</cop><pub>Lippincott Williams &amp; Wilkins</pub><pmid>33565773</pmid><doi>10.1097/DSS.0000000000002473</doi><tpages>6</tpages></addata></record>
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subjects Aged
Biopsy - statistics & numerical data
Carcinoma, Basal Cell - diagnosis
Carcinoma, Basal Cell - pathology
Carcinoma, Basal Cell - surgery
Carcinoma, Squamous Cell - diagnosis
Carcinoma, Squamous Cell - pathology
Carcinoma, Squamous Cell - surgery
Dermatology
Female
Frozen Sections - statistics & numerical data
Humans
Keratosis, Actinic - diagnosis
Keratosis, Actinic - pathology
Keratosis, Actinic - surgery
Life Sciences & Biomedicine
Male
Mohs Surgery - statistics & numerical data
Observer Variation
Reproducibility of Results
Retrospective Studies
Science & Technology
Skin - pathology
Skin Neoplasms - diagnosis
Skin Neoplasms - pathology
Skin Neoplasms - surgery
Surgery
title Diagnostic Biopsy via In-Office Frozen Sections for Clinical Nonmelanoma Skin Cancer
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